Coccidia from the Tiger Salamander, Ambystoma tigrinum, in Northeastern Colorado and in Northern New Mexico

SYNOPSIS. Oocysts of Eimeria ambystomae Saxe, 1955, Eimeria microcapi sp. n., and Eimeria urodela sp. n. are described from the tiger salamander, Ambystoma tigrinum , collected in Colorado and New Mexico. The oocysts of E. ambystomae are ellipsoid, 29.8 × 17.3 (24–38 × 15–25) μm, and the sporocysts lanceolate, 22.6 × 5.4 (16–27 × 5–7) μm. Oocyst and sporocyst residua are present, but not a polar granule and a micropyle. The oocysts and sporocysts of E. microcapi are ellipsoid, measuring respectively 38.1 × 25.3 (35-41 × 23-26) μm and 18.1 × 7.4 (16-19 × 6–8) μm. Oocyst and sporocyst residua, a micropyle (mean 3 μm), and a distinct micropyle cap (2 μm high) are present, but not a polar granule. The oocysts of E. urodela are spheroid, 22.2 (14-26) μm, and the sporocysts lanceolate, 16.3 × 5.8 (12-19 × 4-7) μm. Oocyst and sporocyst residua are present, but a polar granule and a micropyle are absent.     

Some Microscopical Observations of Functioning Sieve Tubes of Heracleum using Nomarski Optics

The study of isolated phloem in Heracleum has been extendedto intact functioning sieve tubes. Techniques of phloem dissectioncombined with Nomarski interference optics have been developedto permit useful visual observations, photomicrography, andciné photographs of sieve tubes which are apparentlynormal. In these preparations, plastids and organelles calledby us ‘marker particles’ are visible in rapid bouncingmotion, and the state of dispersal of these particles is relatedto the amount of damage done to the preparations. The movement of the marker particles and their subsequent fixationshows that they are apparently attached to or restrained byan invisible network in situ. The network is very sensitiveto disturbance and readily collapses around the sieve platesto form slime plugs upon damage to the sieve element. The markerparticles do not move through the cell nor across sieve platesin mature Heracleum. In young cells cyclosis is observable alongthe periphery and this suggests that a vacuole may then be present.In undamaged mature cells there was evidence neither of a vacuolenor of trans-cellular tubules of any size optically detectable. The motion of the particles was greater than Brownian movementand appeared to be under some physiological control. Their movementprobably indicated the presence of an operating transport phenomenon,either because solution was moving past them in the sieve tubeor because they were themselves attached to a contractile networkactively in pulsatory motion. Nearby companion and parenchymacells showed normal cytoplasmic streaming. Proposed mechanisms of translocation involving cytoplasmic streamingdo not seem to be applicable to the phloem of Heracleum. Themovement of the marker particles seemed to agree best with amechanism of ‘activated’ mass flow.     

CONSIDERATIONS OF THE IDIOGNATHOIDES - DECLINOGNATHODUS - NEOGNATHODUS COMPLEX OF MIDDLE CARBONIFEROUS PLATFORM CONODONTS

An earlier proposed hypothesis by Straka & Lane (1970), suggesting 'Idiognathoides' noduliferus and Idiognathoides sulcatus as the progenitors of a closely related group of Lower Pennsylvanian (Morrowan) conodonts, is here considered as unnecessarily complex and based on insufficient data. An alternative and more simple interpretation is offered based on phylogenetic, ontogenetic, and stratigraphic considerations. It is suggested that the Idiognathoides sulcata (and/or I. opimus)-Idiognathoides sinuatus (and/or I. opimus ) group descended from Gnathodus defectus , and that Neognathodus bassleri was descended from Declinognathodus. Declinognathodus noduliferus and Gnathodus defectus are considered as having shared the common ancestor, Gnathodus girtyi simplex.     

Nucleoside diphosphate kinase from lily pollen

Nucleoside diphosphate kinase was a predominantly soluble enzymein lily pollen (Lilium longiflorum, var. Ace), and very littleenzyme activity was associated with the mitochondrial fraction.GTP was the preferred substrate when ADP was the second substrate.The enzyme was purified 18-fold to a specific activity of 7µmoles/min/mg protein. ¹This study was supported by grant GB-8764 from the U.S. NationalScience Foundation. (Received October 5, 1970; )     

Ribosomes,G-factor and Siomycin

G-factor interacts with the 50S ribo-somal subunit at a site which is distinct from the peptidyl transferase centre and which is inactivated by siomycin.     

Antigenic Heterogeneity of Human IgD Immunoglobulins

SUBCLASSES of the three major classes of human immunoglobulins, IgG, IgA and IgM, are recognized: four of IgG are well defined^1,2 and at least two of IgA^3–5 and two of IgM^6,7 have been demonstrated. This communication presents evidence for the existence of an antigenic heterogeneity in the heavy chains of IgD, which may also be indicative of subclasses within this class of immunoglobulin.     

中国蝶类新种小志Ⅳ

本文记述国产眼蝶科(Satyridae)的一个新属Sinonympha与它的一个模式种Sinonympha amoena(新种),这一蝶类最早是笔者于1939年7月在我国四川省西北部的杂谷脑(理县)发见的。为欲较全面地了解它们在分类系统上的亲缘关系,又于1963年和1964年在原产地采集了大量的成虫标本,并于1965—1966年在北京饲养了它的幼期。 新华新眼蝶属Sinonympha新属 新属属征 新华新眼蝶属Sinonympha(新属)与Coenonympha Hbner(1819)较为近似,但是某些形态特征和生物学特性(包括幼期)则与Ypthima Hbner(1818),OeneisHbner(1819)以及Mycalesis Hbner(1818)等属的种类互有相似之处,现将本新属的主要特征列述于下:     

Storage Polysaccharide in Coccidial Sporozites after Excystation and Penetration of Cells

SYNOPSIS. Eimeria acervulina, E. necatrix , and E. meleagrimitis sporozoites were examined for carbohydrates by cytochemical methods during dormancy, after excystation, and after penetration of cells. The only carbohydrate found was amylopectin, a homogeneous polymer of glucose. It was distributed in 3 regions: (a) in front of the anterior refractile globule, (b) around the nucleus, and (c) behind the posterior refractile globule. The relative amounts decreased after excystation and penetration of cells until only small amounts remained around the nucleus. The quantity of amylopectin decreased following excystation from 30.0-36.7 to 9.4-13.3 μg glucose/10⁶ oocysts. Over a 6 yr period of storage at 4 C, there was a decrease in the quantity of amylopectin in dormant sporozoites of E. acervulina from 33.3 μg glucose/10⁶ oocysts at 3 mos to 1.5 μg at 6 years. Coincidentally, 3 month- and 1 year-old oocysts of E. acervulina produced patent infections in chicks with a dosage of 5 × 10⁴ oocysts, but only a few of the oocysts that had been stored for 2 years were infective; a dosage of 2 × 10⁶ oocysts was necessary to produce a patent infection. Oocysts which had been stored 6 years did not produce a patent infection.
It was concluded that amylopectin is the energy source for excystation and subsequent penetration of cells. Small amounts of amylopectin are used during dormancy and, when the content in the sporozoite falls below a certain level, the sporozoites lack sufficient energy to infect cells.     

The Polyunsaturated Fatty Acids of Marine and Freshwater Cryptomonads1

SYNOPSIS Fatty acids were examined of photosynthetic and non-photosynthetic marine and freshwater cryptomonads cultured as photoauxotrophs, photoheterotrophs and heterotrophs at various incubation temperatures and constant light intensity. Photo-synthetic marine and freshwater forms contained octadecatrienoic, octadecatetraenoic, eicosapentaenoic and docosahexaenoic (all-cis, ω3 acids) as the major polyunsaturates, and a freshwater heterotroph contained mostly the octadecatrienoic acid. The polar lipids of a marine, photosynthetic form, Cryptomonas sp., included the usual thylakoid membrane lipids of the chloroplasts of eukaryotic, photosynthetic cells: galactosyl diglycerides, phosphatidyl glycerol and a sulfolipid. Also present were 2 choline-containing phospholipids: phosphatidyl choline and an unknown. Ninhydrin-positive and inositol-containing lipids were not detected. Octadecatetraenoic acid comprised 75% of the total fatty acids of the monogalactosyl diglyceride fraction. The phosphatidyl glycerol was acylated mostly by ω13 trans-hexadecaenoic acid and the eicosapentaenoic acid. Evolutionary relationships of cryptomonads as mirrored in lipid composition are discussed.